Acute Hypobaric Hypoxia Causes Alterations in Acetylcholine-Mediated Signaling Through Varying Expression of Muscarinic Receptors in the Prefrontal Cortex and Cerebellum of Rats' Brain.

IF 1.6 4区 医学 Q4 BIOPHYSICS High altitude medicine & biology Pub Date : 2024-10-08 DOI:10.1089/ham.2023.0146
Narendra Kumar Sharma, Mansi Srivastava, Tikam Chand Dakal, Vipin Ranga, Pawan Kumar Maurya
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Abstract

Sharma, Narendra Kumar, Mansi Srivastava, Tikam Chand Dakal, Vipin Ranga, and Pawan Kumar Maurya. Acute hypobaric hypoxia (HH) causes alterations in acetylcholine-mediated signaling through varying expression of muscarinic receptors in the PFC and cerebellum of rats' brain. High Alt Med Biol. 00:00-00, 2024. Background: Muscarinic receptor (CHRM) proteins are G-protein-associated acetylcholine receptors found in neuronal membranes. Five major subtypes, CHRM1-CHRM5, modulate acetylcholine in central nervous system signaling cascades. CHRM1, CHRM3, and CHRM5 are linked to Gαq/Gα11 proteins, whereas CHRM2 and CHRM4 are linked to Gαi/Gαo proteins. Objective: Limited research has been conducted to explore the impact of HH on CHRM gene expressions. It is caused by low oxygen availability at high altitudes, which impairs neurotransmission, cognitive performance, and physiological functions. Previous studies have shown that exposure to hypoxia leads to a reduction in CHRM receptors, which in turn causes alteration in signal transduction, physiological responses, cognitive deficits, and mood alterations. Method: In the present study, we have used semiquantitative PCR to measure muscarinic receptor gene expression after 6, 12, and 24 hours of HH exposure at 25,000 feet using a decompression chamber in rat brain's PFC and cerebellum. Result: We have found that CHRM1-CHRM5 downregulated after acute exposure to hypoxia until 12 hours, and then, the expression level of these receptors increased to 24 hours when compared with 12 hours in PFC. All subtypes have shown a similar pattern in PFC regions under hypoxia exposure. On the other hand, these receptors have shown altered expression at different time points in the cerebellum. CHRM1 and CHRM4 acutely downregulated, CHRM2 and CHRM5 downregulated, while CHRM3 upregulated after hypoxia exposure. Conclusion: Our study, for the first time, has shown the altered expressions of muscarinic receptors under temporal hypoxia exposure. The altered expression pattern has shown an association with acclimatization and protection against necrosis due to hypoxia. This study may pave further investigations for understanding and addressing the cognitive, behavioral, and physiological impacts of hypoxia and therapeutic development.

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急性低压缺氧通过改变大鼠大脑前额叶皮层和小脑中肌肉卡因受体的表达导致乙酰胆碱介导的信号转导发生改变
Sharma, Narendra Kumar, Mansi Srivastava, Tikam Chand Dakal, Vipin Ranga, and Pawan Kumar Maurya.急性低压缺氧(HH)通过大鼠大脑PFC和小脑中毒蕈碱受体的不同表达引起乙酰胆碱介导的信号转导的改变。High Alt Med Biol.背景:毒蕈碱受体(CHRM)蛋白是神经元膜上的G蛋白相关乙酰胆碱受体。五个主要亚型(CHRM1-CHRM5)在中枢神经系统信号级联中调节乙酰胆碱。CHRM1、CHRM3 和 CHRM5 与 Gαq/Gα11 蛋白相连,而 CHRM2 和 CHRM4 则与 Gαi/Gαo 蛋白相连。目的:有关 HH 对 CHRM 基因表达影响的研究十分有限。高海拔地区氧气供应不足会损害神经传递、认知能力和生理功能。以往的研究表明,暴露于低氧环境会导致 CHRM 受体减少,进而引起信号转导、生理反应、认知障碍和情绪改变。研究方法在本研究中,我们使用半定量 PCR 技术测量了在 25000 英尺高空使用减压舱暴露于 HH 6、12 和 24 小时后大鼠大脑全脑和小脑中毒蕈碱受体基因的表达。研究结果我们发现,在急性暴露于缺氧环境 12 小时之前,CHRM1-CHRM5 下调,然后,与 12 小时相比,这些受体在 PFC 中的表达水平上升至 24 小时。在缺氧条件下,所有亚型受体在 PFC 区域的表达模式相似。另一方面,这些受体在小脑不同时间点的表达也发生了改变。缺氧暴露后,CHRM1 和 CHRM4 急性下调,CHRM2 和 CHRM5 下调,而 CHRM3 上调。结论我们的研究首次显示了在时间性缺氧暴露下毒蕈碱受体表达的改变。这种表达模式的改变与适应性和保护细胞免受缺氧导致的坏死有关。这项研究为进一步了解和解决缺氧对认知、行为和生理的影响以及治疗方法的开发铺平了道路。
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来源期刊
High altitude medicine & biology
High altitude medicine & biology 医学-公共卫生、环境卫生与职业卫生
CiteScore
3.80
自引率
9.50%
发文量
44
审稿时长
>12 weeks
期刊介绍: High Altitude Medicine & Biology is the only peer-reviewed journal covering the medical and biological issues that impact human life at high altitudes. The Journal delivers critical findings on the impact of high altitude on lung and heart disease, appetite and weight loss, pulmonary and cerebral edema, hypertension, dehydration, infertility, and other diseases. It covers the full spectrum of high altitude life sciences from pathology to human and animal ecology.
期刊最新文献
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